4jwd

Crystal structure of the substrate binding domain of E.coli DnaK in complex with bovine Bac7(15-28)

Method: X-RAY DIFFRACTION Dmax: 83.9 Å Quality: REASONABLE

1. Protein Identity and Related Structures Protein Identity & Related Structures

Chaperone protein DnaK

Escherichia coli

UniProt P0A6Y8

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 389–607 Fragment:unp residues 389-607 Cathelicidin-3 × 1 (P19661) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.4;292 K;2.2 M ammonium sulfate, 0.1 M citric acid pH 4.4, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.95 Å R-free 0.217
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 389–607 Fragment:unp residues 389-607 Cathelicidin-3 × 1 (P19661) SO4 SULFATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.4;292 K;2.2 M ammonium sulfate, 0.1 M citric acid pH 4.4, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.95 Å R-free 0.217

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

52 other PDB entries and 124 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DNAK_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–219; UniProt 389–607 Author chain B; PDBConstruct 1–219; UniProt 389–607

Cathelicidin-3

OrganismNot specified

UniProt P19661

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain D; UniProt 159–172 Fragment:unp residues 159-172 Chaperone protein DnaK × 1 (P0A6Y8) SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.4;292 K;2.2 M ammonium sulfate, 0.1 M citric acid pH 4.4, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.95 Å R-free 0.217
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 159–172 Fragment:unp residues 159-172 Chaperone protein DnaK × 1 (P0A6Y8) SO4 SULFATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.4;292 K;2.2 M ammonium sulfate, 0.1 M citric acid pH 4.4, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.95 Å R-free 0.217

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

3 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CTHL3_BOVIN
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 1–14; UniProt 159–172 Author chain D; PDBConstruct 1–14; UniProt 159–172

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 4jwd

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4jwd
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4jwd
Deposition date deposition_date2013-03-27
Structure title titleCrystal structure of the substrate binding domain of E.coli DnaK in complex with bovine Bac7(15-28)
Keywords keywordschaperone, peptide binding, antimicrobial peptide, PEPTIDE BINDING PROTEIN, CHAPERONE-Antibiotic complex; CHAPERONE/Antibiotic
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier26.01
Radius of gyration Rg (electron density) rg_electron25.51
Forward intensity I(0) i041754200.00
Molecular weight molecular_weight47930.0 kDa
Excluded volume excluded_volume59453 ų
Envelope volume envelope_volume78924 ų
Hydration-shell volume shell_volume26844 ų
Envelope diameter envelope_diameter88.8
Shell Rg shell_rg31.33
Envelope Rg envelope_rg25.68
Shape Rg shape_rg25.49
Total Rg total_rg26.24
Total atoms total_atoms3355
Residues n_residues439
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax83.9
Rg (real space) rg_real25.99
Rg uncertainty (real space) rg_real_error0.68
I(0) (real space) i0_real4.1750e+07
I(0) uncertainty (real space) i0_real_error6.0270e+05
Rg (reciprocal space) rg_reciprocal25.99
I(0) (reciprocal space) i0_reciprocal41750000.0000
Solution quality estimate total_estimate0.6450
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary31.6
Skewness Skewness skewness0.310
Kurtosis Kurtosis kurtosis-0.376
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6573000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.910; Stabil: 0.999; Sysdev: 0.221; Positv: 1.000; Valcen: 0.993; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

CATH v4.4 (4 domains)

Domain ID domain_id4jwdA01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology34 — Substrate Binding Domain Of DNAk; Chain A, domain 1
Homologous superfamily homologous superfamily10 — Substrate Binding Domain Of DNAk; Chain A, domain 1
Domain ID domain_id4jwdA02
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1270 — Substrate Binding Domain Of Dnak; Chain:A; Domain 2
Homologous superfamily homologous superfamily10
Domain ID domain_id4jwdB01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology34 — Substrate Binding Domain Of DNAk; Chain A, domain 1
Homologous superfamily homologous superfamily10 — Substrate Binding Domain Of DNAk; Chain A, domain 1
Domain ID domain_id4jwdB02
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1270 — Substrate Binding Domain Of Dnak; Chain:A; Domain 2
Homologous superfamily homologous superfamily10

8. Citations (1)

9. Files and Curves (10)